NDC product
POWDER · Hubei Haosun Pharmaceutical Co., Ltd.
NDC 14778-0808 · Hubei Haosun Pharmaceutical Co., Ltd.
Key facts
| Product NDC | 14778-0808 |
|---|---|
| Nonproprietary name | NILOTINIB HYDROCHLORIDE MONOHYDRATE |
| Substances | NILOTINIB HYDROCHLORIDE MONOHYDRATE |
| Dosage form | POWDER |
| Labeler | Hubei Haosun Pharmaceutical Co., Ltd. |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | May 14, 2025 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: